Wide nose
Symptom Information:
Symptom ID: | HPO:0000445 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the nose(HPO:0000366) Abnormal nasal morphology(HPO:0005105) Wide nose(HPO:0000445) MedDRA: |
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Database Frequency: | 190 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
12q14 microdeletion syndrome | (Orphanet:94063) |
14q11.2 microdeletion syndrome | (Orphanet:261120) |
15q24 microdeletion syndrome | (Orphanet:94065) |
16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
16p13.11 microdeletion syndrome | (Orphanet:261236) |
17p13.3 microduplication syndrome | (Orphanet:217385) |
1q21.1 microdeletion syndrome | (Orphanet:250989) |
20p12.3 microdeletion syndrome | (Orphanet:261295) |
22q11.2 microduplication syndrome | (Orphanet:1727) |
3q13 microdeletion syndrome | (Orphanet:1621) |
49,XXXXY syndrome | (Orphanet:96264) |
8p23.1 microdeletion syndrome | (Orphanet:251071) |
8p23.1 microduplication syndrome | (Orphanet:251076) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
ADULT syndrome | (Orphanet:978) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Acrodysostosis | (Orphanet:950) |
Acromegaly | (Orphanet:963) |
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Ascher syndrome | (Orphanet:1253) |
Aspartylglucosaminuria | (Orphanet:93) |
Atrioventricular defect - blepharophimosis -radial defects | (Orphanet:1352) |
Auriculoocular anomalies - cleft lip | (Orphanet:71270) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive chorioretinopathy-microcephaly | (Orphanet:2518) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
Axenfeld-Rieger syndrome | (Orphanet:782) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Barber-Say syndrome | (Orphanet:1231) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
CHARGE syndrome | (Orphanet:138) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
Camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia | (Orphanet:1321) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Central diabetes insipidus | (Orphanet:178029) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Charlie M syndrome | (Orphanet:1406) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Cloverleaf skull - multiple congenital anomalies | (Orphanet:93267) |
Coffin-Lowry syndrome | (Orphanet:192) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cold-induced sweating syndrome | (Orphanet:157820) |
Craniodiaphyseal dysplasia | (Orphanet:1513) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Craniorhiny | (Orphanet:157832) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Deafness - onychodystrophy | (Orphanet:3231) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | (Orphanet:2229) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal monosomy 10p | (Orphanet:1580) |
Distal monosomy 6p | (Orphanet:96125) |
Dysmorphism - short stature - deafness - disorder of sex development | (Orphanet:2282) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Epiphyseal dysplasia - hearing loss - dysmorphism | (Orphanet:1825) |
Ermine phenotype | (Orphanet:999) |
FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES,AND SPONTANEOUS FILTERING BLEBS | (OMIM:601552) |
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation | (Orphanet:1970) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Facial ectodermal dysplasia | (Orphanet:1807) |
Filippi syndrome | (Orphanet:3255) |
Fraser syndrome | (Orphanet:2052) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Frontonasal dysplasia | (Orphanet:250) |
Fryns syndrome | (Orphanet:2059) |
Fucosidosis | (Orphanet:349) |
GCS1-CDG | (Orphanet:79330) |
GM1 gangliosidosis | (Orphanet:354) |
Geleophysic dysplasia | (Orphanet:2623) |
Genitopatellar syndrome | (Orphanet:85201) |
German syndrome | (Orphanet:2077) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
Hennekam syndrome | (Orphanet:2136) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
Hydrocephaly - low insertion umbilicus | (Orphanet:2184) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Hypertelorism, Teebi type | (Orphanet:1519) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus | (Orphanet:3044) |
Intellectual deficit - short stature - hypertelorism | (Orphanet:3074) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy | (Orphanet:2958) |
Intellectual deficit, X-linked, Siderius type | (Orphanet:85287) |
Isotretinoin-like syndrome | (Orphanet:2306) |
Jacobsen syndrome | (Orphanet:2308) |
Juberg-Hayward syndrome | (Orphanet:2319) |
Jung-Wolff-Back-Stahl syndrome | (Orphanet:2321) |
Keipert syndrome | (Orphanet:2662) |
Keutel syndrome | (Orphanet:85202) |
Langer-Giedion syndrome | (Orphanet:502) |
Laurin-Sandrow syndrome | (Orphanet:2378) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Lethal recessive chondrodysplasia | (Orphanet:1423) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35 | (OMIM:615162) |
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM | (OMIM:616033) |
MULTIPLE SYNOSTOSES SYNDROME 2 | (OMIM:610017) |
Marshall syndrome | (Orphanet:560) |
Megalencephaly | (Orphanet:2477) |
Metaphyseal acroscyphodysplasia | (Orphanet:1240) |
Microcephalic primordial dwarfism, Alazami type | (Orphanet:319671) |
Microcephaly - brachydactyly - kyphoscoliosis | (Orphanet:3433) |
Microcephaly - intellectual deficit - phalangeal and neurological anomalies | (Orphanet:137658) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Microcephaly - seizures - intellectual deficit - heart disease | (Orphanet:2519) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Microcornea-myopic chorioretinal atrophy-telecanthus syndrome | (Orphanet:369970) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Mietens syndrome | (Orphanet:2557) |
Monosomy 13q14 | (Orphanet:1587) |
Monosomy 18p | (Orphanet:1598) |
Mosaic trisomy 14 | (Orphanet:1703) |
Mosaic trisomy 8 | (Orphanet:96061) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
Muckle-Wells syndrome | (Orphanet:575) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Neonatal adrenoleukodystrophy | (Orphanet:44) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Osteocraniostenosis | (Orphanet:2763) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY | (OMIM:602342) |
Patent arterial duct | (Orphanet:706) |
Paternal 20q13.2q13.3 microdeletion syndrome | (Orphanet:261304) |
Pentasomy X | (Orphanet:11) |
Pierre Robin syndrome - faciodigital anomaly | (Orphanet:2888) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Pyruvate dehydrogenase deficiency | (Orphanet:765) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Rhizomelic dysplasia, Patterson-Lowry type | (Orphanet:2831) |
Ring chromosome 10 | (Orphanet:1438) |
Say-Field-Coldwell syndrome | (Orphanet:3133) |
Scheie syndrome | (Orphanet:93474) |
Sclerosteosis | (Orphanet:3152) |
Short rib-polydactyly syndrome, Verma-Naumoff type | (Orphanet:93271) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Smith-Magenis syndrome | (Orphanet:819) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Summitt syndrome | (Orphanet:3210) |
Symptomatic form of Coffin-Lowry syndrome in female carriers | (Orphanet:276630) |
Syndromic diarrhea | (Orphanet:84064) |
TEMPLE SYNDROME | (OMIM:616222) |
TEMPLE-BARAITSER SYNDROME | (OMIM:611816) |
TENORIO SYNDROME | (OMIM:616260) |
TRICHOHEPATOENTERIC SYNDROME 2 | (OMIM:614602) |
Trisomy 17p | (Orphanet:261290) |
Trisomy 1q | (Orphanet:261344) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
W syndrome | (Orphanet:2804) |
Waardenburg-Shah syndrome | (Orphanet:897) |
Weaver-Williams syndrome | (Orphanet:3448) |
Wiedemann-Steiner syndrome | (Orphanet:319182) |
Williams syndrome | (Orphanet:904) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |
Zechi-Ceide syndrome | (Orphanet:217017) |
Zellweger syndrome | (Orphanet:912) |
Zimmermann-Laband syndrome | (Orphanet:3473) |